Canonical Allele Identifier: CA368858509
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917419A>G , CM000669.2:g.107917419A>G GRCh38
NC_000007.13:g.107557864A>G , CM000669.1:g.107557864A>G GRCh37
NC_000007.12:g.107345100A>G NCBI36
NG_008045.1:g.31279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1193A>G MANE Select ENSP00000205402.3:p.Glu398Gly
ENST00000205402.9:c.1193A>G ENSP00000205402.3:p.Glu398Gly
ENST00000415325.5:c.*867A>G ENSP00000402593.1:n.*867A>G
ENST00000417551.5:c.1193A>G ENSP00000390667.1:p.Glu398Gly
ENST00000437604.6:c.1049A>G ENSP00000387542.2:p.Glu350Gly
ENST00000440410.5:c.1124A>G ENSP00000417016.1:p.Glu375Gly
NM_000108.4:c.1193A>G NP_000099.2:p.Glu398Gly
NM_001289750.1:c.896A>G NP_001276679.1:p.Glu299Gly
NM_001289751.1:c.1124A>G NP_001276680.1:p.Glu375Gly
NM_001289752.1:c.1049A>G NP_001276681.1:p.Glu350Gly
NM_000108.5:c.1193A>G MANE Select NP_000099.2:p.Glu398Gly